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Progesterone (PROG) Rapid Quantitative Test Kit (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref SUPF123024

by Shenzhen Superbio Technology Co., Ltd.

Identity

Trade Name
Progesterone (PROG) Rapid Quantitative Test Kit (FIA) EUDAMED
Device Name
Progesterone (PROG) Rapid Quantitative Test Kit (FIA) EUDAMED
Model / Reference
SUPF123024 EUDAMED

Identifiers

Primary DI / UDI-DI
06974521002277 EUDAMED
Basic UDI-DI
B-06974521002277 EUDAMED
EMDN Code
W0102160399 FERTILITY/PREGNANCY RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Progesterone (PROG) Rapid Quantitative Test Kit (FIA) by Shenzhen Superbio Technology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000024149
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 9fcba2c3-d0f5-4d53-bc46-206a473e6407 61 fields · synced Jun 18, 2026